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MIM:612242 - CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME
Xenbase Genes: pten, bmpr1a
Human Disease Resource: MIM
MONDO:0012830 - chromosome 10q23 deletion syndrome |
MONDO:0017380 - juvenile polyposis syndrome |
MONDO:0019190 - juvenile polyposis of infancy |
DOID:0060389 - chromosome 10q23 deletion syndrome |